Healthcare Utilization and Outcomes of FinESS Treatment in the Office

Completed · Not applicable

Conditions studied: Rhinosinusitis

In brief

A prospective, nonrandomized trial to evaluate postoperative healthcare resource utilization after maxillary balloon antrostomy using FinESS Sinus Treatment in the physician's office.

Key facts

Study ID

NCT00986830

Run by

Entellus Medical, Inc.

People needed

74

Starts

2009-09-01

Expected to finish

2012-09-01

Last updated by the study team

2020-10-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older
• Male or female subjects
• Diagnosis of rhinosinusitis (CT radiographic evidence and medical evaluation)
• Willing to comply with protocol requirements
• Able to provide consent

You may not qualify if…

• Hemophilia
• Cystic fibrosis
• Ciliary dysfunction
• Severe septal deviation causing obstruction of the ostiomeatal unit
• Pregnant females

Where it is running

• Central California ENT — Fresno, California, United States
• South Denver ENT and Allergy — Denver, Colorado, United States
• ENT and Allergy Associates — Trumbull, Connecticut, United States
• NorthShore University — Evanston, Illinois, United States
• Advanced ENT and Allergy — Louisville, Kentucky, United States
• St. Cloud Ear, Nose and Throat — Saint Cloud, Minnesota, United States
• Coastal Ear, Nose and Throat Associates — New Bern, North Carolina, United States
• Midwest Ear, Nose and Throat — Sioux Falls, South Dakota, United States
• Holston Medical Center — Kingsport, Tennessee, United States
• Austin Ear, Nose and Throat — Austin, Texas, United States
• Texas Sinus Center — Boerne, Texas, United States
• The Snoring Center — Dallas, Texas, United States
• Advanced Otolaryngology PC — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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